FDA Inspection 1169788 — Martin K. Dineen, M.D.

Martin K. Dineen, M.D. — FEI 3003576224

The FDA completed an inspection of Martin K. Dineen, M.D. on May 5, 2022 in Daytona Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 5, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Daytona Beach, FL (United States)

Additional Details

Clinical Investigator (CI)